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aspirin + metoprolol + atorvastatin + rosuvastatin + clopidogrel + ticagrelor

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Small Molecules
Administration
Oral
01

Overview

This combination consists of six pharmaceuticals: **aspirin**, **metoprolol**, **atorvastatin**, **rosuvastatin**, **clopidogrel**, and **ticagrelor**. - **Aspirin** is an antiplatelet agent that irreversibly inhibits cyclooxygenase-1, reducing thromboxane A2 production and thereby limiting platelet aggregation. - **Metoprolol** is a selective beta-1 adrenergic receptor blocker that reduces heart rate, cardiac output, and blood pressure, primarily used in hypertension, angina, and heart failure. - **Atorvastatin** and **rosuvastatin** are HMG-CoA reductase inhibitors (statins) that lower LDL cholesterol and overall cardiovascular risk by inhibiting cholesterol biosynthesis. - **Clopidogrel** and **ticagrelor** are P2Y12 receptor antagonists, inhibiting ADP-induced platelet aggregation for prevention of atherothrombotic events. Clopidogrel is a prodrug requiring metabolic activation, while ticagrelor is a direct-acting, reversible inhibitor. Combining these agents could theoretically provide comprehensive management for patients at very high cardiovascular risk (e.g., those with ischemic heart disease, post-acute coronary syndrome, post-PCI/CABG, or major risk factors), encompassing anti-thrombotic, beta-blockade, and dual statin lipid-lowering mechanisms, though the use of two statins and two P2Y12 inhibitors concurrently is non-standard and could greatly increase adverse effect risk. Such a combination is not described as a standard therapy or marketed as a finished product in major guidelines or literature[2][4][6].

02

Targets

PGHS-1 (Prostaglandin G/H Synthase 1)HMGCR (3-hydroxy-3-methylglutaryl-coenzyme A reductase)ADRB1 (β1)ADRB2 (β2)PTGS2 (Prostaglandin-Endoperoxide Synthase 2)

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